Shenzhen Mindray Bio-Meidcal Electronics Co., Ltd.
Shenzhen Mindray Bio-Meidcal Electronics Co., Ltd. holds FDA 510(k) medical device clearances, first cleared 2012, most recent 2022.
Top product codes for Shenzhen Mindray Bio-Meidcal Electronics Co., Ltd.
Recent clearances by Shenzhen Mindray Bio-Meidcal Electronics Co., Ltd.
- K221267 — VS 8 Vital Signs Monitor, VS 8A Vital Signs Monitor, VS 9 Vital Signs Monitor
- K222754 — ViewMate Multi Ultrasound System
- K202785 — Resona R9,Resona R9 Exp,Resona R9 Pro,Resona R9S, Nuewa R9,Nuewa R9 Exp,Nuewa R9 Pro,Nuewa R9S,Resona 7,Resona 7CV,Resona 7EXP,Resona 7S, Resona 7OB,Resona 7PRO,Imagyn 7,Resona Y Diagnostic Ultrasound System
- K173369 — DC-30/DC-32/DC-28/DC-26/DC-25 Diagnostic Ultrasound System
- K171233 — Resona 7/Resona 7CV/Resona 7EXP/Resona 7S/Resona 7OB Diagnostic Ultrasound System
- K170712 — Accutorr 7/VS-900 Vital Signs Monitor
- K143195 — Passport Series Patient Monitors (including Passport 17M, Passport 12M and T1)
- K132036 — HYPERVISOR CENTRAL MONITORING SYSTEM (INCLUDING TELEMETRY MONITORING SYSTEM, TMS-6016)
- K113632 — DP-5 DIGITAL ULTRASONIC DIAGNOSTIC IMAGING SYSTEM DP-7 DIGITAL ULTRASONIC DIAGNOSTIC IMAGING SYSTEM
Data sourced from openFDA. This site is unofficial and independent of the FDA.